Goichi Miyazumi

FDA Filings

This page includes the latest FDA filings for Goichi Miyazumi. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3004138517
FEI Number3004138517
NameGOICHI MIYAZUMI
Owner & OperatorNIPRO CORPORATION
Contact Address3-9-3, Honjo-Nishi, Kita-Ku --
Osaka JP-27 Osaka 531-8510 JP
Official Correspondent
  • Tadao Kobayashi
  • 81-6-63756739-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3150 NW 107 AVE..
MIAMI, FL 33172 US
Establishment TypeManufacture Medical Device

Registration Number3000247873
FEI Number3000247873
NameGOICHI MIYAZUMI
Owner & OperatorNIPRO CORPORATION
Contact Address3-9-3, Honjo-Nishi, Kita-Ku --
Osaka JP-27 Osaka 531-8510 JP
Official Correspondent
  • Tadao Kobayashi
  • 81-6-63756739-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3150 NW 107 AVE. MIAMI
Doral, FL 33172 US
Establishment TypeExport Device to the United States But Perform No Other Operation on Device

Registration Number3016250252
FEI Number3016250252
NameGOICHI MIYAZUMI
Owner & OperatorNIPRO CORPORATION
Contact Address3-9-3, Honjo-Nishi, Kita-Ku --
Osaka JP-27 Osaka 531-8510 JP
Official Correspondent
  • Tadao Kobayashi
  • 81-6-63756739-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3150 NW 107 AVE.
Miami, FL 33172 US
Establishment TypeManufacture Medical Device

Registration Number9611446
FEI Number3002807725
NameGOICHI MIYAZUMI
Owner & OperatorNIPRO CORPORATION
Contact Address3-9-3, Honjo-Nishi, Kita-Ku --
Osaka JP-27 Osaka 531-8510 JP
Official Correspondent
  • Tadao Kobayashi
  • 81-6-63756739-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3150 NW 107 AVE.
MIAMI, FL 33172 US
Establishment Type
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)

Registration Number3002533790
FEI Number3002533790
NameGOICHI MIYAZUMI
Owner & OperatorNIPRO MEDICAL LTDA
Contact AddressAvenida Nipro, 451 Regiao Norte
SOROCABA BR-SP Sao Paulo 18087-127 BR
Official Correspondent
  • Claudio A Ghiotti Jr.
  • 55-15-32387330-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3150 NW 107 AVE..
MIAMI, FL 33172 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
GOICHI MIYAZUMI [NIPRO CORPORATION]
Surdial DX Hemodialysis System and Accessories2019-09-08
GOICHI MIYAZUMI [NIPRO CORPORATION]
Surdial DX Hemodialysis System and Accessories2019-09-08
GOICHI MIYAZUMI [NIPRO CORPORATION]
Ophthalmic Needle2017-05-31
GOICHI MIYAZUMI [NIPRO CORPORATION]
Ophthalmic Needle2017-05-31
GOICHI MIYAZUMI [NIPRO CORPORATION]
NIPRO SAFETOUCH IV CATHETER2017-03-21
GOICHI MIYAZUMI [NIPRO CORPORATION]
NIPRO SAFETOUCH IV CATHETER winged2017-03-21
GOICHI MIYAZUMI [NIPRO CORPORATION]
NIPRO Cellentia Dialyzer2017-03-21
GOICHI MIYAZUMI [NIPRO CORPORATION]
Safe Touch PSV Winged Infusion Set (with or without filter)2014-09-08
GOICHI MIYAZUMI [NIPRO CORPORATION]
Safe Touch PSV Winged Infusion Set (with or without filter)2014-09-08
GOICHI MIYAZUMI [NIPRO CORPORATION]
ELISIO-09H and 25H.2014-04-22
GOICHI MIYAZUMI [NIPRO CORPORATION]
Nipro SafeTouch PSV Scalp Vein Set with Safety Device2014-02-19
GOICHI MIYAZUMI [NIPRO CORPORATION]
ELISIO-11H, 13H, 15H, 17H, 19H and 21H. ELISIO-11M, 13M, 15M, 17M, 19M and 21M.2014-01-30
GOICHI MIYAZUMI [NIPRO CORPORATION]
Nipro Set - SLIMLINE Blood Tubing Set with Transducer Protector and Priming Set2012-11-22
GOICHI MIYAZUMI [NIPRO CORPORATION]
Scab Remover2010-04-13
GOICHI MIYAZUMI [NIPRO CORPORATION]
NIPRO BioHole Needle with CAPICK2010-04-13
GOICHI MIYAZUMI [NIPRO CORPORATION]
NIPRO Transducer Protector TP-SURE2008-03-31
GOICHI MIYAZUMI [NIPRO CORPORATION]
Sniper Hydrophilic Guidewire2007-11-20
GOICHI MIYAZUMI [NIPRO CORPORATION]
Sniper Hydrophilic Guidewire2007-11-20
GOICHI MIYAZUMI [NIPRO CORPORATION]
AQUALiner2007-11-20
GOICHI MIYAZUMI [NIPRO CORPORATION]
AQUALiner2007-11-20
GOICHI MIYAZUMI [NIPRO CORPORATION]
NIPRO A.V. FISTULA NEEDLE2007-11-15
GOICHI MIYAZUMI [NIPRO CORPORATION]
Nipro Scalp Vein Set2007-11-15
GOICHI MIYAZUMI [NIPRO CORPORATION]
Nipro blood tubing set2007-11-15
GOICHI MIYAZUMI [NIPRO CORPORATION]
Nipro SafeTouch TULIP Safety AVF2007-11-15
GOICHI MIYAZUMI [NIPRO CORPORATION]
Nipro SafeTouch TULIP Safety AVF2007-11-15
GOICHI MIYAZUMI [NIPRO CORPORATION]
Nipro SafeTouch TULIP Safety AVF2007-11-15
GOICHI MIYAZUMI [NIPRO CORPORATION]
Nipro SafeTouch II Gamma2007-11-15
GOICHI MIYAZUMI [NIPRO CORPORATION]
Nipro SafeTouch II Safety AVF2007-11-15
GOICHI MIYAZUMI [NIPRO CORPORATION]
Nipro SafeTouch Safety BCS2007-11-15
GOICHI MIYAZUMI [NIPRO CORPORATION]
Nipro SafeTouch Safety BCS2007-11-15
GOICHI MIYAZUMI [NIPRO MEDICAL LTDA]
NIPRO SAFELET CATH2007-11-01
GOICHI MIYAZUMI [NIPRO CORPORATION]
Nipro Blood Collection Needle2006-11-06
GOICHI MIYAZUMI [NIPRO CORPORATION]
Nipro Blood Collection Needle2006-11-06
GOICHI MIYAZUMI [NIPRO CORPORATION]
Syringe, Piston2006-11-06
GOICHI MIYAZUMI [NIPRO CORPORATION]
Syringe, Piston2006-11-06
GOICHI MIYAZUMI [NIPRO CORPORATION]
Dental Needle2006-07-12
GOICHI MIYAZUMI [NIPRO CORPORATION]
Dental Needle2006-07-12
GOICHI MIYAZUMI [NIPRO CORPORATION]
Nipro Hydrophilic Guidewire2006-03-30
GOICHI MIYAZUMI [NIPRO CORPORATION]
Nipro Hydrophilic Guidewire2006-03-30
GOICHI MIYAZUMI [NIPRO CORPORATION]
NIPRO HYDROPHILIC FOR UR2006-03-30
GOICHI MIYAZUMI [NIPRO CORPORATION]
NIPRO HYDROPHILIC FOR UR2006-03-30
GOICHI MIYAZUMI [NIPRO CORPORATION]
Nipro Hypodermic Needle2005-12-16
GOICHI MIYAZUMI [NIPRO CORPORATION]
Nipro Hypodermic Needle2005-12-16
GOICHI MIYAZUMI [NIPRO CORPORATION]
Needle2004-04-16
GOICHI MIYAZUMI [NIPRO CORPORATION]
Needle2004-04-16
GOICHI MIYAZUMI [NIPRO CORPORATION]
NIPRO SAFELET CATH2001-01-18

Similar & Related FDA Registered Companies

Related Finance Registrations
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.